01 3ACTAVIS LABS FL INC
02 2AIPING PHARM INC
03 2APOTEX
04 2AUROBINDO PHARMA
05 3CHARTWELL RX
06 2INVAGEN PHARMS
07 2JANSSEN RES AND DEV
08 3JUBILANT CADISTA
09 2KVK TECH
10 2MACLEODS PHARMS LTD
11 2NOVAST LABS
12 2OXFORD PHARMS
13 2PAR PHARM INC
14 1PLIVA
15 2PRINSTON INC
16 6RISING
17 3RUBICON RESEARCH
18 1SANDOZ
19 3SUN PHARM INDS LTD
20 2TEVA PHARMS INTL
21 1TONIX
22 2TP ANDA HOLDINGS
23 2TWI PHARMS INC
24 3UNICHEM
25 2WATSON LABS
01 2CAPSULE, EXTENDED RELEASE; ORAL
02 10CAPSULE, EXTENDED RELEASE;ORAL
03 44TABLET;ORAL
04 1TABLET;SUBLINGUAL
01 13DISCN
02 42RX
03 2Blank
01 2AMRIX
02 52CYCLOBENZAPRINE HYDROCHLORIDE
03 2FLEXERIL
04 1TONMYA
01 50No
02 5Yes
03 2Blank
RLD : No
TE Code : AB
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1989-05-03
Application Number : 71611
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2006-02-03
Application Number : 71611
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 7.5MG
Approval Date : 2006-02-03
Application Number : 71611
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1991-11-27
Application Number : 73143
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1991-11-19
Application Number : 72854
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2006-02-03
Application Number : 72854
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : FLEXERIL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17821
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : FLEXERIL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17821
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : AMRIX
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 15MG
Approval Date : 2007-02-01
Application Number : 21777
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : AMRIX
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 30MG
Approval Date : 2007-02-01
Application Number : 21777
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
